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Desonide API Manufacturers & Suppliers

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Commercial-scale Suppliers

Distributor
Produced in  World
|

Employees: 200+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
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CEP
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USDMF
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MSDS
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BSE/TSE

All certificates

GMP
CEP
USDMF
MSDS
BSE/TSE
CoA
Distributor
Produced in  China
|

Employees: 50+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: USDMF
|
ISO9001
|
CoA

All certificates

USDMF
ISO9001
CoA
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Producer
Produced in  India
|

Employees: 200+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
MSDS
|
BSE/TSE
|
CoA

All certificates

GMP
MSDS
BSE/TSE
CoA
Producer
Produced in  China
|

Employees: 400+

|
Audit Report: Click here for more information on Eurofins audit reports
Certifications: USDMF
|
CoA

All certificates

USDMF
CoA
Producer
Produced in  Slovenia
|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
CoA

All certificates

GMP
CoA
Producer
Produced in  United States
|
Audit Report: Click here for more information on Eurofins audit reports
Certifications: GMP
|
CoA

All certificates

GMP
CoA
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Producer
Produced in  Italy
|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
CoA

All certificates

GMP
CoA
Not active
Producer
Produced in  Italy
|
Audit Report: Click here for more information on Eurofins audit reports
Certifications: GMP
|
USDMF
|
ISO9001
|
CoA

All certificates

GMP
USDMF
ISO9001
CoA
Not active
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Desonide | CAS No: 638-94-8 | GMP-certified suppliers

A medication that provides relief for inflammatory and itchy corticosteroid‑responsive skin conditions, supporting consistent dermatological formulation needs for North American therapeutic markets.

Therapeutic categories

Adrenal Cortex HormonesAnti-Inflammatory AgentsCorticosteroid Hormone Receptor AgonistsCorticosteroidsCorticosteroids, Moderately Potent (Group II)Cytochrome P-450 CYP3A Inducers
Generic name
Desonide
Molecule type
small molecule
CAS number
638-94-8
DrugBank ID
DB01260
Approval status
Approved drug, Investigational drug
ATC code
S01BA11

Primary indications

  • For the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatose

Product Snapshot

  • Desonide is a topical small-molecule corticosteroid available in multiple cutaneous and ophthalmic formulations including creams, lotions, ointments, gels, solutions, and foams
  • It is used for corticosteroid‑responsive inflammatory and pruritic dermatologic conditions
  • It is approved in the US and Canada, with both approved and investigational statuses noted across formulations

Clinical Overview

Desonide (CAS 638-94-8) is a nonfluorinated topical corticosteroid classified within the 21‑hydroxysteroid family, used for inflammatory and pruritic manifestations of corticosteroid‑responsive dermatoses. It is applied to reduce cutaneous inflammation in conditions where local glucocorticoid activity is therapeutically appropriate.

Pharmacologically, desonide functions as a moderately potent corticosteroid intended for dermatologic use. Its therapeutic activity reflects anti‑inflammatory, antipruritic, and vasoconstrictive effects mediated through glucocorticoid receptor agonism. After topical administration, the drug binds cytosolic glucocorticoid receptors, and the resulting complex translocates to the nucleus to modulate gene transcription. A key downstream pathway involves induction of phospholipase A2 inhibitory proteins, or lipocortins, which limit the liberation of arachidonic acid from membrane phospholipids. This reduces the biosynthesis of prostaglandins and leukotrienes, thereby diminishing inflammatory mediator production at the site of application.

Systemic absorption is typically low when applied to intact skin, but uptake increases with occlusion, compromised epidermal barriers, large treatment areas, or prolonged use. Metabolic pathways are primarily hepatic, consistent with corticosteroid biotransformation, and the drug is known to interact with cytochrome P450 3A systems as both a substrate and inducer. Distribution and elimination parameters are influenced by the low systemic exposures achieved with proper topical use.

Safety considerations center on local corticosteroid effects such as skin atrophy, irritation, telangiectasia, and potential hypothalamic‑pituitary‑adrenal axis suppression when used extensively or under conditions that increase absorption. Use near the eyes requires caution due to the theoretical risk of elevated intraocular pressure or cataract formation reported with corticosteroids. Long‑term continuous application is generally avoided unless clinically justified.

Desonide is available in various topical formulations globally, including creams, lotions, gels, and ointments. For API procurement, sourcing should prioritize material identity verification, impurity profile control aligned with ICH expectations, and consistent potency to support formulation reproducibility and regulatory compliance.

Identification & chemistry

Generic name Desonide
Molecule type Small molecule
CAS 638-94-8
UNII J280872D1O
DrugBank ID DB01260

Pharmacology

SummaryDesonide is a topical corticosteroid that modulates inflammatory and pruritic responses by activating cytosolic glucocorticoid receptors and altering downstream gene transcription. Its activity is primarily attributed to induction of lipocortins, which inhibit phospholipase A2 and reduce production of prostaglandins and leukotrienes. The drug’s pharmacologic effect centers on suppressing key inflammatory pathways in corticosteroid‑responsive dermatologic conditions.
Mechanism of actionLike other topical corticosteroids, desonide has anti-inflammatory, antipruritic and vasoconstrictive properties. The drug binds to cytosolic glucocorticoid receptors. This complex migrates to the nucleus and binds to genetic elements on the DNA. This activates and represses various genes. However corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2.
PharmacodynamicsDesonide is a synthetic nonfluorinated corticosteroid for topical dermatologic use. The corticosteroids constitute a class of primarily synthetic steroids used topically as anti-inflammatory and antipruritic agents.
Targets
TargetOrganismActions
Glucocorticoid receptorHumansagonist

ADME / PK

AbsorptionTopical corticosteroids can be absorbed from normal intact skin, inflammation and/or other disease processes in the skin may increase percutaneous absorption.

Formulation & handling

  • Desonide is a small‑molecule corticosteroid formulated primarily for topical and ophthalmic use, relying on semi‑solid or liquid vehicles to address its low aqueous solubility.
  • Its moderate lipophilicity (LogP ~1.9) supports incorporation into creams, ointments, lotions, and emulsions, with excipient selection focused on maintaining uniform dispersion and preventing crystallization.
  • Being a solid steroidal API, it is generally stable but requires protection from excessive heat and light, with attention to oxidative stability in emulsified and solution‑based systems.

Regulatory status

LifecycleMost U.S. patents for the API have already expired, with the final protection ending in 2028, indicating a late‑stage lifecycle. In the U.S. and Canada, the market is largely mature, with remaining exclusivity expected to conclude in the near term.
MarketsCanada, US
Supply Chain
Supply chain summaryDesonide is supplied by numerous manufacturers and packagers, indicating that the original product’s role has diminished and the market is largely supported by established generic producers. Branded and generic formulations are available in the US and Canada, reflecting broad regional penetration. Most core patents have expired, with only later‑expiring formulation‑related patents remaining, supporting the presence of existing generics alongside limited protected presentations.

Desonide is a type of Dermatics


Dermatics is a prominent subcategory within the pharmaceutical Active Pharmaceutical Ingredient (API) sector. It focuses on the development and production of APIs specifically designed for dermatological applications. These APIs play a crucial role in the formulation of various pharmaceutical products used in the treatment of skin disorders, including creams, ointments, gels, and lotions.

Dermatics APIs are meticulously developed to address specific dermatological conditions such as acne, psoriasis, eczema, fungal infections, and other related ailments. The APIs used in these formulations are carefully selected for their therapeutic efficacy, safety, and compatibility with the skin.

Manufacturers of Dermatics APIs employ rigorous quality control measures to ensure the purity, potency, and stability of their products. These APIs undergo extensive testing to meet stringent regulatory standards and pharmacopoeial guidelines. Additionally, the production processes adhere to Good Manufacturing Practices (GMP) to guarantee consistent quality and minimize the risk of contamination.

With the increasing demand for advanced dermatological treatments, Dermatics APIs are subject to continuous research and development. Newer APIs are being explored to enhance efficacy, minimize side effects, and improve patient compliance. The field of Dermatics APIs is characterized by innovation, as researchers strive to develop novel compounds and delivery systems that address unmet therapeutic needs.

In summary, Dermatics APIs are a vital component of pharmaceutical formulations used in the treatment of skin disorders. They undergo stringent quality control measures and are constantly evolving to provide effective and safe dermatological solutions.


Desonide (Dermatics), classified under Dermatological Agents


Dermatological agents are a vital category of pharmaceutical active pharmaceutical ingredients (APIs) used in the formulation of various skincare and dermatology products. These APIs are specifically designed to target and treat skin conditions, offering effective solutions for a wide range of dermatological concerns.

Dermatological agents encompass a diverse array of compounds, including corticosteroids, antifungal agents, antibacterials, retinoids, and immunomodulators. Each API within this category possesses unique properties and mechanisms of action, enabling them to address specific skin-related issues.

Corticosteroids, for instance, are potent anti-inflammatory agents commonly used in the treatment of skin conditions like eczema, psoriasis, and dermatitis. Antifungal agents, on the other hand, combat fungal infections such as athlete's foot or ringworm. Antibacterials are effective against bacterial infections, while retinoids promote skin cell turnover and treat acne and photoaging. Immunomodulators regulate the immune response, providing relief from conditions like atopic dermatitis.

The development and application of dermatological APIs involve rigorous research, clinical trials, and regulatory compliance. These APIs are typically integrated into topical creams, ointments, gels, and lotions, ensuring targeted delivery to the affected areas of the skin.

Dermatological agents play a crucial role in the management and treatment of various skin disorders. By harnessing the therapeutic properties of these APIs, pharmaceutical companies can develop innovative skincare products that cater to the diverse needs of individuals seeking effective dermatological solutions.



Desonide API manufacturers & distributors

Compare qualified Desonide API suppliers worldwide. We currently have 8 companies offering Desonide API, with manufacturing taking place in 6 different countries. Use the table below to review supplier type, countries of origin, certifications, product portfolio and GMP audit availability.

SupplierTypeCountryProduct originCertificationsPortfolio
Producer
Italy United States CoA, GMP104 products
Producer
Italy Italy CoA, GMP, ISO9001, USDMF58 products
Producer
India India BSE/TSE, CoA, GMP, MSDS166 products
Producer
China China CoA, USDMF14 products
Producer
Slovenia Slovenia CoA, GMP81 products
Distributor
United States World BSE/TSE, CEP, CoA, GMP, MSDS, USDMF441 products
Producer
Italy Italy CoA, GMP47 products
Distributor
China China CoA, ISO9001, USDMF762 products

When sending a request, specify which Desonide API quality you need: for example EP (Ph. Eur.), USP, JP, BP, or another pharmacopoeial standard, as well as the required grade (base, salt, micronised, specific purity, etc.).

Use the list above to find high-quality Desonide API suppliers. For example, you can select GMP, FDA or ISO certified suppliers. Visit our help page to learn more about sourcing APIs via Pharmaoffer.

Frequently asked questions about Desonide API


Sourcing

What matters most when sourcing GMP-grade Desonide?
Key factors include confirming GMP compliance and meeting US and Canadian regulatory requirements. Suppliers should demonstrate consistent quality and documentation that align with regional standards. It is also important to verify reliable supply from established generic manufacturers and be aware of any remaining formulation‑related patent protections.
Which documents are typically required when sourcing Desonide API?
Request the core API documentation set: CoA (8 companies), GMP (6 companies), USDMF (4 companies), ISO9001 (2 companies), MSDS (2 companies). Confirm versions and validity dates match the destination market to avoid delays in qualification.
Which manufacturers are known to produce Desonide API?
Known or reported manufacturers for Desonide: Sinoway industrial Co.,Ltd, LGM Pharma, Gonane Pharma. Evaluate their GMP history, scale, and regional coverage before requesting dossiers or allocating demand.
How can I request quotes for Desonide API from GMP suppliers?
Submit quote requests through the supplier listings with your specs and required documents (specifications, target volume, delivery timeline, and destination). Providing consistent details upfront speeds comparable offers and clarifies technical feasibility.
Is a GMP audit report available for Desonide manufacturers?
Audit reports may be requested for Desonide: 3 GMP audit reports available. Confirm the scope and recency of any audit before relying on it for qualification decisions.
How many suppliers offer Desonide API on Pharmaoffer?
Reported supplier count for Desonide: 8 verified suppliers. Filter listings by certifications, regions, and delivery options to match your qualification plan.
Which countries are known to manufacture Desonide API?
Production countries reported for Desonide: China (2 producers), Italy (2 producers), India (1 producer). Knowing the manufacturing geography helps anticipate logistics lead times and import compliance needs.
Which certifications do suppliers of Desonide usually hold?
Common certifications for Desonide suppliers: CoA (8 companies), GMP (6 companies), USDMF (4 companies), ISO9001 (2 companies), MSDS (2 companies). Always verify issuing authorities and expiry dates when reviewing audit packages.

Technical

What is Desonide (CAS 638-94-8) used for?
Desonide is a moderate‑potency topical corticosteroid used to treat inflammatory and pruritic manifestations of corticosteroid‑responsive dermatoses. It reduces cutaneous inflammation and itching through glucocorticoid receptor–mediated suppression of inflammatory mediator production.
Which therapeutic class does Desonide fall into?
Desonide belongs to the following therapeutic categories: Adrenal Cortex Hormones, Anti-Inflammatory Agents, Corticosteroid Hormone Receptor Agonists, Corticosteroids, Corticosteroids, Moderately Potent (Group II). This positioning helps teams compare alternative APIs, anticipate pharmacology expectations, and align early research priorities.
What conditions is Desonide mainly prescribed for?
The primary indications for Desonide: For the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatose. These use cases frame the target patient populations and help prioritize formulation and safety evaluations.
How does Desonide work?
Like other topical corticosteroids, Desonide has anti-inflammatory, antipruritic and vasoconstrictive properties. The drug binds to cytosolic glucocorticoid receptors. This complex migrates to the nucleus and binds to genetic elements on the DNA. This activates and represses various genes. However corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2.
What should someone know about the safety or toxicity profile of Desonide?
Desonide has a safety profile consistent with topical corticosteroids, with local effects such as skin atrophy, irritation, and telangiectasia possible, especially with prolonged use or application to sensitive areas. Systemic absorption is usually low but can increase with occlusion, damaged skin, large surface areas, or extended treatment, which may suppress the hypothalamic‑pituitary‑adrenal axis. Use near the eyes requires caution because corticosteroids can contribute to elevated intraocular pressure or cataract formation. Long‑term continuous application is generally avoided unless clinically necessary.
What are important formulation and handling considerations for Desonide as an API?
Desonide’s low aqueous solubility and moderate lipophilicity favor incorporation into semi‑solid or liquid topical vehicles, with excipients selected to maintain uniform dispersion and prevent crystallization. Protection from excessive heat and light is recommended to preserve stability, and oxidative stability should be managed in emulsified or solution formulations. Because topical corticosteroids can be absorbed through intact skin, formulation should also support consistent dosing to limit unintended increases in percutaneous absorption.
Is Desonide a small molecule?
Desonide is classified as a small molecule. That classification shapes process design, impurity profiling, and analytical control strategies.
Are there special stability concerns for oral Desonide?
Desonide is a generally stable solid steroid, with key concerns centered on protection from excessive heat and light. Its low aqueous solubility would require formulation approaches that maintain uniform dispersion and prevent crystallization. As with emulsified or solution‑based systems, controlling oxidative conditions is important if any non‑solid oral vehicle were used.

Regulatory

Where is Desonide approved or in use globally?
Desonide is reported as approved in the following major regions: Canada, US. Understanding geographic coverage informs regulatory filings, supply planning, and risk assessments before escalating procurement.
What’s the regulatory and patent landscape for Desonide right now?
Desonide is described as being regulated for use in Canada and the United States. Patent information is not included in the provided context, so only its regulatory presence in these markets can be noted.

Pharmaoffer

How does Pharmaoffer’s Smart Sourcing Service help with Desonide procurement?
Pharmaoffer's Smart Sourcing Service coordinates compliant suppliers, documentation, and competitive quotes for Desonide. It centralizes outreach, follow-ups, and document validation to shorten procurement timelines.
Is Desonide included in the PRO Data Insights coverage?
PRO Data Insights coverage for Desonide: 279 verified transactions across 100 suppliers and 67 buyers worldwide. Use the dataset to benchmark suppliers and monitor regulatory activity where available.
Where can I access the API market report for Desonide?
Market report availability for Desonide: Report Available. The report highlights demand trends, pricing drivers, and supplier landscape insights for procurement planning.